Non-Additive Variation
variation that is not predictably transmitted from parent to offspring; different contributions to a given trait are given by each allele
Dominance
genetic phenomena where one allele can override the effect of the other allele on the same chromosome
Epistasis
the interaction between genes, influencing a phenotype
Gene X Environment
Genotype can have no impact on the phenotype, unless certain environmental conditions are satisfied; these are hard to identify, as finding large numbers of participants that have all been exposed to the same environment is challenging/impossible
Non-Additive Dominance
different contributions are made by each allele to the phenotype
Additive Dominance
each allele contributes the same amount to the trait
Non-Additive Epistasis
different contributions from different loci, altering the phenotype
Additive Epistasis
each loci provides the same contribution to the phenotype, increasing the phenotype by a factor instead of a constant value
Omnigenic Model
hypothesis proposing that all genes expressed in a cell impact the expression of a given trait
Core Gene
genes having a direct impact on the expression of a trait, described by the omnigenic model
Peripheral Genes
genes that have an indirect impact on the expression of a trait and explain more heritability than the core genes, as described by the omnigenic model
Silent Genes
genes that aren’t expressed and therefore cannot have an impact on the expression of a trait, according to the omnigenic model
Medullary Thymic Epithelial Cells (mTEC) Cell
cells found in the thymus that are essential for developing tolerance to self-antigens; express all self-proteins, with any T cells that bind directed to undergo apoptosis or develop into T regulatory cells to prevent autoimmunity
Non-Modifiable Risk
a risk factor that cannot be changed, such as family history, age of childbirth, …
Modifiable Risk
a risk factor for a condition that can be changed by the individual, such as alcohol intake, BMI, smoking, …
Cis-Regulatory Module, CRM
regions of non-coding DNA regulating the transcription of neighbouring genes, involved in regulatory networks to control morphogenesis, anatomical development, and other aspects of evolutionary biology; normally regulate gene expression by binding transcription factors
Promoter
DNA sequence able to initiate transcription of an RNA transcript from a DNA template downstream
Type I Promoter
promoters with a focal start site, with all RNA transcripts from that promoter starting at exactly the same nucleotide position
Type II Promoter
promoter with a less well defined start site, with RNA transcripts starting in a general region; CpG islands are more common; housekeeping genes are generally under these promoters
Type III Promoter
promoters with broad start locations, containing many CpG islands; developmental genes are usually under these promoters
CpG Island
a cytosine nucleotide followed immediately by a guanine nucleotide; able to be methylated